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   <subfield code="a">New supraglottic airway with built-in pressure indicator decreases postoperative pharyngolaryngeal symptoms: a randomized controlled trial</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[David Wong, Amanda Tam, Vanita Mehta, Raviraj Raveendran, Waleed Riad, Frances Chung]</subfield>
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   <subfield code="a">Un nouveau dispositif supraglottique avec un indicateur intégré de pression diminue les symptômes pharyngo-laryngés postopératoires: un essai randomisé contrôlé</subfield>
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   <subfield code="a">Purpose: Excessive supraglottic airway cuff pressure increases postoperative pharyngolaryngeal symptoms such as sore throat, dysphonia, and dysphagia. A new supraglottic airway, AES Ultra CPV™ (CPV), has a built-in intracuff pressure indicator. We hypothesized that using the CPV would reduce postoperative symptoms when compared with the LMA Classic™ (LMA) without intracuff pressure guidance. Methods: Ambulatory patients undergoing general anesthesia were randomized to either CPV or LMA. A size 3/4/5 was inserted according to manufacturer guidelines. Nitrous oxide was not used. In the LMA Group, the cuff was inflated according to manufacturer's guidelines. In the CPV Group, a CPV was inserted and the cuff inflated until the indicator was in the green zone (30-44mmHg). Intracuff pressures were measured at five minutes and 20min post-insertion in both groups. The primary outcome was the incidence of pharyngolaryngeal symptoms, defined as sore throat, dysphonia, and/or dysphagia at one, two, and/or 24hr postoperatively. Continuous data were compared using Student's t test and categorical data were analyzed using Chi square analysis. Results: The study included 170 patients, 85 per group. The mean (SD) intracuff pressure in the CPV group was significantly lower [44 (4) mmHg] than in the LMA Group [87 (37) mmHg]; P&lt;0.001. The incidence of pharyngolaryngeal symptoms was significantly lower in the CPV Group than in the LMA Group (26% vs 49%; P=0.002). The absolute risk reduction was 24%, and the number-needed-to-treat was 4.3. Conclusion: The incidence of postoperative pharyngolaryngeal symptoms in the CPV Group with a cuff pressure-guided strategy was significantly lower than in the LMA Group with standard practice. (Clinical trial registration number: NCT01800344).</subfield>
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